欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4534/001
药品名称Gaviscon Double Action Tablets
活性成分
    • calcium carbonate 187.5 mg
    • sodium bicarbonate 106.5 mg
    • sodium alginate 250.0 mg
剂型Chewable tablet
上市许可持有人Reckitt Benckiser Healthcare (UK) Limited Dansom Lane Hull HU8 7DS United Kingdom
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
      PL 00063/0157 - 0018
    • Germany (DE)
      Gaviscon Double Action 250mg/ 106,5mg/ 187,5mg Kautabletten
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Greece (GR)
    • Cyprus (CY)
      GAVISCON DOUBLE ACTION TABS
    • Czechia (CZ)
      Gaviscon Double Action tablety
    • Slovakia (SK)
      Gaviscon Double Action tablety
许可日期2010/05/18
最近更新日期2024/04/23
药物ATC编码
    • A02BX Other drugs for peptic ulcer and gastro-oesophageal reflux disease (GORD)
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase